Reacción #44989

Ecuación de reacción

Trans-4-(methoxycarbonyl)cyclohexanecarboxylic acid

dimethylamine hydrochloride

1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride

triethylamine

→

methyl trans-4-[(dimethylamino)carbonyl]-cyclohexanecarboxylate

Rendimiento 87.7%

Disolventes

chloroform

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturacooling
2. 2
   Extracciónthe mixture is extracted with chloroform
3. 3
   LavadoThe organic layer is washed with 10% hydrochloric acid, saturated aqueous sodium hydrogen carbonate solution and saturated brine successively
4. 4
   Secadodried over sodium sulfate
5. 5
   ConcentraciónThe solvent is concentrated under reduced pressure
6. 6
   Otrothe resulting residue is purified by silica gel column chromatography (eluent: chloroform, followed by chloroform/methanol=20/1)

Procedimiento

Trans-4-(methoxycarbonyl)cyclohexanecarboxylic acid (20.0 g) obtained in Reference Example 1(2) is dissolved in chloroform (200 ml), and thereto are added dimethylamine hydrochloride (10.5 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (24.7 g) and triethylamine (26.0 g) under ice-cooling. The mixture is then stirred at room temperature for 17 hours. Ice-water is poured to the reaction solution and the mixture is extracted with chloroform. The organic layer is washed with 10% hydrochloric acid, saturated aqueous sodium hydrogen carbonate solution and saturated brine successively and dried over sodium sulfate. The solvent is concentrated under reduced pressure and the resulting residue is purified by silica gel column chromatography (eluent: chloroform, followed by chloroform/methanol=20/1) to give methyl trans-4-[(dimethylamino)carbonyl]-cyclohexanecarboxylate (20.1 g).

Fuente